182 related articles for article (PubMed ID: 35652341)
21. Whole-Exome Sequencing Analyses Support a Role of Vitamin D Metabolism in Ischemic Stroke.
Xie Y; Acosta JN; Ye Y; Demarais ZS; Conlon CJ; Chen M; Zhao H; Falcone GJ
Stroke; 2023 Mar; 54(3):800-809. PubMed ID: 36762557
[TBL] [Abstract][Full Text] [Related]
22. Genetic Risk of Primary Aldosteronism and Its Contribution to Hypertension: A Cross-Ancestry Meta-Analysis of Genome-Wide Association Studies.
Naito T; Inoue K; Sonehara K; Baba R; Kodama T; Otagaki Y; Okada A; Itcho K; Kobuke K; Kishimoto S; Yamamoto K; ; Morisaki T; Higashi Y; Hinata N; Arihiro K; Hattori N; Okada Y; Oki K
Circulation; 2023 Apr; 147(14):1097-1109. PubMed ID: 36802911
[TBL] [Abstract][Full Text] [Related]
23. Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis.
Uimari O; Rahmioglu N; Nyholt DR; Vincent K; Missmer SA; Becker C; Morris AP; Montgomery GW; Zondervan KT
Hum Reprod; 2017 Apr; 32(4):780-793. PubMed ID: 28333195
[TBL] [Abstract][Full Text] [Related]
24. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
Liu C; Kraja AT; Smith JA; Brody JA; Franceschini N; Bis JC; Rice K; Morrison AC; Lu Y; Weiss S; Guo X; Palmas W; Martin LW; Chen YD; Surendran P; Drenos F; Cook JP; Auer PL; Chu AY; Giri A; Zhao W; Jakobsdottir J; Lin LA; Stafford JM; Amin N; Mei H; Yao J; Voorman A; ; ; ; ; Larson MG; Grove ML; Smith AV; Hwang SJ; Chen H; Huan T; Kosova G; Stitziel NO; Kathiresan S; Samani N; Schunkert H; Deloukas P; ; Li M; Fuchsberger C; Pattaro C; Gorski M; ; Kooperberg C; Papanicolaou GJ; Rossouw JE; Faul JD; Kardia SL; Bouchard C; Raffel LJ; Uitterlinden AG; Franco OH; Vasan RS; O'Donnell CJ; Taylor KD; Liu K; Bottinger EP; Gottesman O; Daw EW; Giulianini F; Ganesh S; Salfati E; Harris TB; Launer LJ; Dörr M; Felix SB; Rettig R; Völzke H; Kim E; Lee WJ; Lee IT; Sheu WH; Tsosie KS; Edwards DR; Liu Y; Correa A; Weir DR; Völker U; Ridker PM; Boerwinkle E; Gudnason V; Reiner AP; van Duijn CM; Borecki IB; Edwards TL; Chakravarti A; Rotter JI; Psaty BM; Loos RJ; Fornage M; Ehret GB; Newton-Cheh C; Levy D; Chasman DI
Nat Genet; 2016 Oct; 48(10):1162-70. PubMed ID: 27618448
[TBL] [Abstract][Full Text] [Related]
25. Non-replication study of a genome-wide association study for hypertension and blood pressure in African Americans.
Kidambi S; Ghosh S; Kotchen JM; Grim CE; Krishnaswami S; Kaldunski ML; Cowley AW; Patel SB; Kotchen TA
BMC Med Genet; 2012 Apr; 13():27. PubMed ID: 22494468
[TBL] [Abstract][Full Text] [Related]
26. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
Surendran P; Drenos F; Young R; Warren H; Cook JP; Manning AK; Grarup N; Sim X; Barnes DR; Witkowska K; Staley JR; Tragante V; Tukiainen T; Yaghootkar H; Masca N; Freitag DF; Ferreira T; Giannakopoulou O; Tinker A; Harakalova M; Mihailov E; Liu C; Kraja AT; Fallgaard Nielsen S; Rasheed A; Samuel M; Zhao W; Bonnycastle LL; Jackson AU; Narisu N; Swift AJ; Southam L; Marten J; Huyghe JR; Stančáková A; Fava C; Ohlsson T; Matchan A; Stirrups KE; Bork-Jensen J; Gjesing AP; Kontto J; Perola M; Shaw-Hawkins S; Havulinna AS; Zhang H; Donnelly LA; Groves CJ; Rayner NW; Neville MJ; Robertson NR; Yiorkas AM; Herzig KH; Kajantie E; Zhang W; Willems SM; Lannfelt L; Malerba G; Soranzo N; Trabetti E; Verweij N; Evangelou E; Moayyeri A; Vergnaud AC; Nelson CP; Poveda A; Varga TV; Caslake M; de Craen AJ; Trompet S; Luan J; Scott RA; Harris SE; Liewald DC; Marioni R; Menni C; Farmaki AE; Hallmans G; Renström F; Huffman JE; Hassinen M; Burgess S; Vasan RS; Felix JF; ; Uria-Nickelsen M; Malarstig A; Reily DF; Hoek M; Vogt T; Lin H; Lieb W; ; Traylor M; Markus HF; ; Highland HM; Justice AE; Marouli E; ; Lindström J; Uusitupa M; Komulainen P; Lakka TA; Rauramaa R; Polasek O; Rudan I; Rolandsson O; Franks PW; Dedoussis G; Spector TD; ; Jousilahti P; Männistö S; Deary IJ; Starr JM; Langenberg C; Wareham NJ; Brown MJ; Dominiczak AF; Connell JM; Jukema JW; Sattar N; Ford I; Packard CJ; Esko T; Mägi R; Metspalu A; de Boer RA; van der Meer P; van der Harst P; ; Gambaro G; Ingelsson E; Lind L; de Bakker PI; Numans ME; Brandslund I; Christensen C; Petersen ER; Korpi-Hyövälti E; Oksa H; Chambers JC; Kooner JS; Blakemore AI; Franks S; Jarvelin MR; Husemoen LL; Linneberg A; Skaaby T; Thuesen B; Karpe F; Tuomilehto J; Doney AS; Morris AD; Palmer CN; Holmen OL; Hveem K; Willer CJ; Tuomi T; Groop L; Käräjämäki A; Palotie A; Ripatti S; Salomaa V; Alam DS; Shafi Majumder AA; Di Angelantonio E; Chowdhury R; McCarthy MI; Poulter N; Stanton AV; Sever P; Amouyel P; Arveiler D; Blankenberg S; Ferrières J; Kee F; Kuulasmaa K; Müller-Nurasyid M; Veronesi G; Virtamo J; Deloukas P; ; Elliott P; ; Zeggini E; Kathiresan S; Melander O; Kuusisto J; Laakso M; Padmanabhan S; Porteous D; Hayward C; Scotland G; Collins FS; Mohlke KL; Hansen T; Pedersen O; Boehnke M; Stringham HM; ; Frossard P; Newton-Cheh C; ; Tobin MD; Nordestgaard BG; ; ; ; ; Caulfield MJ; Mahajan A; Morris AP; Tomaszewski M; Samani NJ; Saleheen D; Asselbergs FW; Lindgren CM; Danesh J; Wain LV; Butterworth AS; Howson JM; Munroe PB
Nat Genet; 2016 Oct; 48(10):1151-1161. PubMed ID: 27618447
[TBL] [Abstract][Full Text] [Related]
27. Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.
Hoffmann TJ; Ehret GB; Nandakumar P; Ranatunga D; Schaefer C; Kwok PY; Iribarren C; Chakravarti A; Risch N
Nat Genet; 2017 Jan; 49(1):54-64. PubMed ID: 27841878
[TBL] [Abstract][Full Text] [Related]
28. Genetically Predicted Blood Pressure and Risk of Atrial Fibrillation.
Hyman MC; Levin MG; Gill D; Walker VM; Georgakis MK; Davies NM; Marchlinski FE; Damrauer SM
Hypertension; 2021 Feb; 77(2):376-382. PubMed ID: 33390040
[TBL] [Abstract][Full Text] [Related]
29. Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood.
Zheng Y; Huang T; Wang T; Mei Z; Sun Z; Zhang T; Ellervik C; Chai JF; Sim X; van Dam RM; Tai ES; Koh WP; Dorajoo R; Saw SM; Sabanayagam C; Wong TY; Gupta P; Rossing P; Ahluwalia TS; Vinding RK; Bisgaard H; Bønnelykke K; Wang Y; Graff M; Voortman T; van Rooij FJA; Hofman A; van Heemst D; Noordam R; Estampador AC; Varga TV; Enzenbach C; Scholz M; Thiery J; Burkhardt R; Orho-Melander M; Schulz CA; Ericson U; Sonestedt E; Kubo M; Akiyama M; Zhou A; Kilpeläinen TO; Hansen T; Kleber ME; Delgado G; McCarthy M; Lemaitre RN; Felix JF; Jaddoe VWV; Wu Y; Mohlke KL; Lehtimäki T; Wang CA; Pennell CE; Schunkert H; Kessler T; Zeng L; Willenborg C; Peters A; Lieb W; Grote V; Rzehak P; Koletzko B; Erdmann J; Munz M; Wu T; He M; Yu C; Lecoeur C; Froguel P; Corella D; Moreno LA; Lai CQ; Pitkänen N; Boreham CA; Ridker PM; Rosendaal FR; de Mutsert R; Power C; Paternoster L; Sørensen TIA; Tjønneland A; Overvad K; Djousse L; Rivadeneira F; Lee NR; Raitakari OT; Kähönen M; Viikari J; Langhendries JP; Escribano J; Verduci E; Dedoussis G; König I; Balkau B; Coltell O; Dallongeville J; Meirhaeghe A; Amouyel P; Gottrand F; Pahkala K; Niinikoski H; Hyppönen E; März W; Mackey DA; Gruszfeld D; Tucker KL; Fumeron F; Estruch R; Ordovas JM; Arnett DK; Mook-Kanamori DO; Mozaffarian D; Psaty BM; North KE; Chasman DI; Qi L
Eur J Epidemiol; 2020 Jul; 35(7):685-697. PubMed ID: 32383070
[TBL] [Abstract][Full Text] [Related]
30. Imputation-based assessment of next generation rare exome variant arrays.
Martin AR; Tse G; Bustamante CD; Kenny EE
Pac Symp Biocomput; 2014; ():241-52. PubMed ID: 24297551
[TBL] [Abstract][Full Text] [Related]
31. Genomics of hypertension: the road to precision medicine.
Padmanabhan S; Dominiczak AF
Nat Rev Cardiol; 2021 Apr; 18(4):235-250. PubMed ID: 33219353
[TBL] [Abstract][Full Text] [Related]
32. Advances in the Genetics of Hypertension: The Effect of Rare Variants.
Russo A; Di Gaetano C; Cugliari G; Matullo G
Int J Mol Sci; 2018 Feb; 19(3):. PubMed ID: 29495593
[TBL] [Abstract][Full Text] [Related]
33. Genetic architecture of ambulatory blood pressure in the general population: insights from cardiovascular gene-centric array.
Tomaszewski M; Debiec R; Braund PS; Nelson CP; Hardwick R; Christofidou P; Denniff M; Codd V; Rafelt S; van der Harst P; Waterworth D; Song K; Vollenweider P; Waeber G; Zukowska-Szczechowska E; Burton PR; Mooser V; Charchar FJ; Thompson JR; Tobin MD; Samani NJ
Hypertension; 2010 Dec; 56(6):1069-76. PubMed ID: 21060006
[TBL] [Abstract][Full Text] [Related]
34. Replication of European hypertension associations in a case-control study of 9,534 African Americans.
Kaur H; Crawford DC; Liang J; Benchek P; ; Zhu X; Kallianpur AR; Bush WS
PLoS One; 2021; 16(11):e0259962. PubMed ID: 34793544
[TBL] [Abstract][Full Text] [Related]
35. Adverse Cardiovascular Outcomes and Antihypertensive Treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies.
McDonough CW; Warren HR; Jack JR; Motsinger-Reif AA; Armstrong ND; Bis JC; House JS; Singh S; El Rouby NM; Gong Y; Mychaleckyj JC; Rotroff DM; Benavente OR; Caulfield MJ; Doria A; Pepine CJ; Psaty BM; Glorioso V; Glorioso N; Hiltunen TP; Kontula KK; Arnett DK; Buse JB; Irvin MR; Johnson JA; Munroe PB; Wagner MJ; Cooper-DeHoff RM
Clin Pharmacol Ther; 2021 Sep; 110(3):723-732. PubMed ID: 34231218
[TBL] [Abstract][Full Text] [Related]
36. White Blood Cells and Blood Pressure: A Mendelian Randomization Study.
Siedlinski M; Jozefczuk E; Xu X; Teumer A; Evangelou E; Schnabel RB; Welsh P; Maffia P; Erdmann J; Tomaszewski M; Caulfield MJ; Sattar N; Holmes MV; Guzik TJ
Circulation; 2020 Apr; 141(16):1307-1317. PubMed ID: 32148083
[TBL] [Abstract][Full Text] [Related]
37. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.
Warren HR; Evangelou E; Cabrera CP; Gao H; Ren M; Mifsud B; Ntalla I; Surendran P; Liu C; Cook JP; Kraja AT; Drenos F; Loh M; Verweij N; Marten J; Karaman I; Lepe MP; O'Reilly PF; Knight J; Snieder H; Kato N; He J; Tai ES; Said MA; Porteous D; Alver M; Poulter N; Farrall M; Gansevoort RT; Padmanabhan S; Mägi R; Stanton A; Connell J; Bakker SJ; Metspalu A; Shields DC; Thom S; Brown M; Sever P; Esko T; Hayward C; van der Harst P; Saleheen D; Chowdhury R; Chambers JC; Chasman DI; Chakravarti A; Newton-Cheh C; Lindgren CM; Levy D; Kooner JS; Keavney B; Tomaszewski M; Samani NJ; Howson JM; Tobin MD; Munroe PB; Ehret GB; Wain LV; ; ; ; ; ; ; ; ; ; ;
Nat Genet; 2017 Mar; 49(3):403-415. PubMed ID: 28135244
[TBL] [Abstract][Full Text] [Related]
38. Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group.
Irvin MR; Sitlani CM; Floyd JS; Psaty BM; Bis JC; Wiggins KL; Whitsel EA; Sturmer T; Stewart J; Raffield L; Sun F; Liu CT; Xu H; Cupples AL; Tanner RM; Rossing P; Smith A; Zilhão NR; Launer LJ; Noordam R; Rotter JI; Yao J; Li X; Guo X; Limdi N; Sundaresan A; Lange L; Correa A; Stott DJ; Ford I; Jukema JW; Gudnason V; Mook-Kanamori DO; Trompet S; Palmas W; Warren HR; Hellwege JN; Giri A; O'donnell C; Hung AM; Edwards TL; Ahluwalia TS; Arnett DK; Avery CL
Am J Hypertens; 2019 Nov; 32(12):1146-1153. PubMed ID: 31545351
[TBL] [Abstract][Full Text] [Related]
39. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.
He KY; Li X; Kelly TN; Liang J; Cade BE; Assimes TL; Becker LC; Beitelshees AL; Bress AP; Chang YC; Chen YI; de Vries PS; Fox ER; Franceschini N; Furniss A; Gao Y; Guo X; Haessler J; Hwang SJ; Irvin MR; Kalyani RR; Liu CT; Liu C; Martin LW; Montasser ME; Muntner PM; Mwasongwe S; Palmas W; Reiner AP; Shimbo D; Smith JA; Snively BM; Yanek LR; Boerwinkle E; Correa A; Cupples LA; He J; Kardia SLR; Kooperberg C; Mathias RA; Mitchell BD; Psaty BM; Vasan RS; Rao DC; Rich SS; Rotter JI; Wilson JG; ; Chakravarti A; Morrison AC; Levy D; Arnett DK; Redline S; Zhu X
Hum Genet; 2019 Feb; 138(2):199-210. PubMed ID: 30671673
[TBL] [Abstract][Full Text] [Related]
40. Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
Lin BM; Grinde KE; Brody JA; Breeze CE; Raffield LM; Mychaleckyj JC; Thornton TA; Perry JA; Baier LJ; de Las Fuentes L; Guo X; Heavner BD; Hanson RL; Hung YJ; Qian H; Hsiung CA; Hwang SJ; Irvin MR; Jain D; Kelly TN; Kobes S; Lange L; Lash JP; Li Y; Liu X; Mi X; Musani SK; Papanicolaou GJ; Parsa A; Reiner AP; Salimi S; Sheu WH; Shuldiner AR; Taylor KD; Smith AV; Smith JA; Tin A; Vaidya D; Wallace RB; Yamamoto K; Sakaue S; Matsuda K; Kamatani Y; Momozawa Y; Yanek LR; Young BA; Zhao W; Okada Y; Abecasis G; Psaty BM; Arnett DK; Boerwinkle E; Cai J; Yii-Der Chen I; Correa A; Cupples LA; He J; Kardia SL; Kooperberg C; Mathias RA; Mitchell BD; Nickerson DA; Turner ST; Vasan RS; Rotter JI; Levy D; Kramer HJ; Köttgen A; Nhlbi Trans-Omics For Precision Medicine TOPMed Consortium ; TOPMed Kidney Working Group ; Rich SS; Lin DY; Browning SR; Franceschini N
EBioMedicine; 2021 Jan; 63():103157. PubMed ID: 33418499
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
